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AzddMeC

TargetMol
Catalog No. T26726Cas No. 87190-79-2
Alias CS-92, Azidodideoxymethylcytidine, Az-Dcme

AzddMeC (Az-Dcme) is a nucleoside analog with antiviral activity and is an orally active and selective inhibitor of HIV-1 reverse transcriptase and HIV-1 replication.AzddMeC has an EC50 value of 9 nM against HIV-1-infected human PBM cells and 6 nM against HIV-1-infected human macrophages.

AzddMeC

AzddMeC

TargetMol
Purity: 99.62%
Catalog No. T26726Alias CS-92, Azidodideoxymethylcytidine, Az-DcmeCas No. 87190-79-2
AzddMeC (Az-Dcme) is a nucleoside analog with antiviral activity and is an orally active and selective inhibitor of HIV-1 reverse transcriptase and HIV-1 replication.AzddMeC has an EC50 value of 9 nM against HIV-1-infected human PBM cells and 6 nM against HIV-1-infected human macrophages.
Pack SizePriceAvailabilityQuantity
1 mg$71In Stock
5 mg$172In Stock
10 mg$278In Stock
25 mg$562In Stock
50 mg$892In Stock
100 mg$1,490In Stock
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Purity:99.62%
ee:100%
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Product Introduction

Bioactivity
Description
AzddMeC (Az-Dcme) is a nucleoside analog with antiviral activity and is an orally active and selective inhibitor of HIV-1 reverse transcriptase and HIV-1 replication.AzddMeC has an EC50 value of 9 nM against HIV-1-infected human PBM cells and 6 nM against HIV-1-infected human macrophages.
Targets&IC50
HIV-1:9 nM (EC50, Human PBM cells), HIV-1:6 nM (EC50, Human macrophages)
In vitro
AzddMeC emerged as the most potent inhibitor of hepatitis B virus DNA polymerase (50% inhibitor dose, 0.03-0.35 μM). In contrast, cellular DNA polymerase was shown to be resistant to or partially (β) affected by AzddMeC. [4]
In vivo
Following intravenously and orally administered 60 mg/kg AzddMeC to male rhesus monkeys, 3'-azido-3'-deoxythymidine (AZT) was found to be the major metabolite of AzddMeC in monkeys. Serum concentrations of AzddMeC decreased rapidly in a biexponential manner with terminal half-lives ranging from 0.5 to 1.3 h. Total clearance of AzddMeC was 2.00 +/- 0.41 l/h/kg (mean +/- standard deviation) and the fraction of AzddMeC metabolized to AZT was 0.32 +/- 0.05. The total clearance was 2.00 +/- 0.41 l/h/kg (mean +/- standard deviation).[2]
AliasCS-92, Azidodideoxymethylcytidine, Az-Dcme
Chemical Properties
Molecular Weight266.26
FormulaC10H14N6O3
Cas No.87190-79-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 100 mg/mL (375.57 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.7557 mL18.7786 mL37.5573 mL187.7864 mL
5 mM0.7511 mL3.7557 mL7.5115 mL37.5573 mL
10 mM0.3756 mL1.8779 mL3.7557 mL18.7786 mL
20 mM0.1878 mL0.9389 mL1.8779 mL9.3893 mL
50 mM0.0751 mL0.3756 mL0.7511 mL3.7557 mL
100 mM0.0376 mL0.1878 mL0.3756 mL1.8779 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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